Department of Obstetrics and Gynecology, University of Alberta, Edmonton Alberta T5H 3V9, Canada.
McGill University Health Centre Reproductive Centre, 888 de Maisonneuve East, Suite 200, Montreal Quebec H2L 4S8, Canada.
Reprod Biomed Online. 2019 Apr;38(4):520-527. doi: 10.1016/j.rbmo.2018.12.028. Epub 2018 Dec 22.
Does the addition of an aromatase inhibitor improve IVF outcomes in women with endometriomas when pretreating them with gonadotrophin-releasing hormone agonists?
Retrospective two-centre cohort study involving 126 women aged 21-39 years who failed a previous IVF cycle and all subsequent embryo transfers and had sonographic evidence of endometriomas. Women were non-randomly assigned to either 3.75 mg intramuscular depo-leuprolide treatment alone or in combination with 5 mg of oral letrozole daily for 60 days prior to undergoing a fresh IVF cycle. Main outcome measures included clinical pregnancy rate and ongoing pregnancy rate after 24 weeks' gestation.
Prior to treatment, antral follicle count (AFC), basal serum FSH and endometrioma diameter did not differ between groups. After treatment, AFC differed between letrozole and non-letrozole-treated groups (10.3 ± 2.0 versus 6.4 ± 2.5; P = 0.0001), as did mean endometrioma maximum diameter (1.8 ± 0.4 cm versus 3.2 ± 0.8 cm; P = 0.0001). At IVF, the gonadotrophin dose used was significantly lower in letrozole-treated subjects (2079 ± 1119 versus 3716 ± 1314; P = 0.0001), the number of mature oocytes collected was greater (9.1 ± 2.4 versus 4.0 ± 1.7; P = 0.0001), as were the number of two-pronuclear embryos and number of blastocysts. The clinical pregnancy rate was significantly higher in the letrozole-treated group (50% versus 22%, P = 0.003), as was the live birth rate (40% versus 17%, P = 0.008).
The combination of depo-leuprolide acetate monthly for 60 days combined with daily letrozole has better clinical outcomes at IVF in women with endometriomas than depo-leuprolide acetate treatment alone.
在使用促性腺激素释放激素激动剂预处理子宫内膜异位症患者时,添加芳香化酶抑制剂是否会改善体外受精的结局?
回顾性的、涉及 126 名年龄在 21-39 岁之间的妇女的双中心队列研究,这些妇女之前的体外受精周期和所有后续的胚胎移植都失败了,并且有超声证据表明存在子宫内膜异位症。这些妇女被非随机分配到单独使用 3.75mg 肌肉注射的 depot-leuprolide 治疗或 depot-leuprolide 联合每日 5mg 来曲唑治疗组,持续 60 天,然后进行新鲜的体外受精周期。主要的观察指标包括临床妊娠率和 24 周妊娠后的持续妊娠率。
在治疗前,窦卵泡计数(AFC)、基础血清 FSH 和子宫内膜异位症直径在两组之间没有差异。治疗后,来曲唑治疗组和非来曲唑治疗组的 AFC 不同(10.3±2.0 对 6.4±2.5;P=0.0001),平均子宫内膜异位症最大直径也不同(1.8±0.4cm 对 3.2±0.8cm;P=0.0001)。在体外受精时,来曲唑治疗组的促性腺激素剂量明显较低(2079±1119 对 3716±1314;P=0.0001),采集的成熟卵母细胞数量较多(9.1±2.4 对 4.0±1.7;P=0.0001),二原核胚胎数量和囊胚数量也较多。来曲唑治疗组的临床妊娠率明显较高(50%对 22%,P=0.003),活产率也较高(40%对 17%,P=0.008)。
在子宫内膜异位症患者中,每月 depot-leuprolide acetate 治疗 60 天联合每日来曲唑的联合治疗比 depot-leuprolide acetate 单独治疗在体外受精中有更好的临床结局。